Abstract
The development of effective therapies or promising vaccines for AIDS has been a goal of international research for more than a decade but the mutability of the virus and complex pathogenesis of the disease have made these goals extremely elusive. Only recently have traditional chemotherapeutic approaches begun to look promising. As an alternative, a number of groups have been investigating the potential of antiviral RNAs expressed from recombinant viral vectors to form the basis of a gene therapy for the disease. In this paper, I outline several challenges to the efficient deployment of a gene therapy for AIDS, particularly the efficient transduction of heamopoietic cells and their engraftment in a physiologically competent form, and review the current approaches designed to overcome them.
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James, W. (1998). The Use of Ribozymes in Gene Therapy Approaches to AIDS. In: Advances in Hematopoietic Stem Cell Transplantation and Molecular Therapy. Recent Results in Cancer Research, vol 144. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-46836-0_15
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DOI: https://doi.org/10.1007/978-3-642-46836-0_15
Publisher Name: Springer, Berlin, Heidelberg
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